Allele Registry

Canonical Allele Identifier: PA265787

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058746

RCV001753476

ClinVar Variation:

67960

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Asn1722Asp	CA018943 NM_001099404.2:c.5164A>G